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MSX1
GENE/PROTEIN ANTIBODY/ANTIGEN

GENE INFORMATION

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Gene name

 MSX1 (HGNC Symbol)

Synonyms

 HOX7, HYD1, OFC5

Description

 Msh homeobox 1 (HGNC Symbol)

Entrez gene summary

 This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia. [provided by RefSeq, Jul 2008]

Chromosome

 4

Cytoband

 p16.2

Chromosome location (bp)

 4859666 - 4863936

Protein evidence

 Evidence at protein level (all genes)

Ensembl

 ENSG00000163132 (version 78.38)

Entrez gene

 4487

UniProt

 P28360 (UniProt - Evidence at protein level)

neXtProt

 NX_P28360

Antibodypedia

 MSX1 antibodies
 

PROTEIN VIEW

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MSX1-001
  
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)
MSX1-001 ENSP00000372170
ENST00000382723 		P28360
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The Human Protein Atlas project is funded
by the Knut & Alice Wallenberg foundation.